A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589434



Internal ID16030157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4102189..4205501hg38UCSC Ensembl
Innerchr3:4143873..4247185hg19UCSC Ensembl
Innerchr3:4118873..4222185hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38103313
hg19103313
hg18103313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8179n54
Supporting Variantsnssv958032
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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